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Stereoselective electrochemical transformation of 4-substituted cyclohexanones into cis-5-substituted 2,2-dimethoxycyclohexanols
Authors:Elinson  M. N.  Feducovich  S. K.  Dmitriev  D. E.  Dorofeev  A. S.  Vereshchagin  A. N.  Nikishin  G. I.
Affiliation:(1) Russian Academy of Sciences, N. D. Zelinsky Institute of Organic Chemistry, 47 Leninsky prosp., 119991 Moscow, Russian Federation
Abstract:Electrolysis of 4-substituted cyclohexanones in methanol in the presence of sodium halides as mediators in an undivided cell results in the stereoselective formation of cis-5-substituted 2,2-dimethoxycyclohexanols in 70—80% yields.
Keywords:electrolysis  electrochemical oxidation  stereoselectivity  substituted cyclohexanones  mediators  5-substituted 2,2-dimethoxycyclohexanols
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